13 results
rheumatology adultonset aosd hematology hemophagocytic hlh lymphohistiocytosis summary activation arthritis babesia babesiosis cell diagnossi hemeonc histiocytosis hypermagnesemia infectiousdiseases kawasaki kd
Adult-Onset Still's Disease Clinical triad: Fever, Arthralgia/arthritis, Skin rash ± odynophagia + Biological inflammation: Increased neutrophils, Hyperferritinemia, decreased
Adult-Onset Still's ... Differential Diaqnoses ... Complications: MAS ... #Disease #diagnosis ... #management #treatment
Adult-Onset Still's Disease (AOSD) Rare inflammatory disorder of unknown etiology, difficult to diagnose because of heterogenous presentation.
Adult-Onset Still's ... Disease (AOSD) ... #AdultOnset #Stills ... #Disease #AOSD ... #management #treatment
Septic Arthritis - Diagnosis and Management Summary Clinical Exam: hot, swollen, pain with passive AND active ROM
and Management ... ROM +/- fever, chills ... osteomyelitis, trauma ... necrosis, Lyme disease ... 90% sensitive in pediatrics
Adult Onset Still's Disease Systemic inflammation with urticarial rash. Rash: • Nonpruritic, evanescent (correlates with time of
Adult Onset Still's ... mL Gf consider MAS ... Treatment - Mild ... #onset #Stills ... #management
Chagas Disease - American Trypanosomiasis - Diagnosis and Management Summary Chagas disease (American trypanosomiasis) is an infectious
Chagas Disease - ... Trypanosomiasis - Diagnosis ... and Management ... Regimens: • Adult ... #Diagnosis #Management
Kawasaki Disease (KD) - Diagnosis and Management Summary Kawasaki Disease (KD) is the most common vasculitis of
Kawasaki Disease ... rarely occurs in adults ... #rheumatology #pediatrics ... #diagnossi #management ... #treatment
Macrophage Activation Syndrome (MAS) Classified among the secondary or acquired forms of haemophagocytic lymphohistiocytosis (sHLH) What? A subset of
arthritis (sJIA) • Adult-onset ... Still disease ... Treatment: • Corticosteroids ... Activation #Syndrome #Diagnosis ... #Management #Hematology
Hemophagocytic Lymphohistiocytosis (HLH) Pathophysiology: Triggering factor (infection,...)→Activation of CD8 T cells (IFN-y) → Excessive activation of macrophages
• Autoimmune diseases ... : SLE+++, Adult-onset ... Still disease, ... Unknown cause Treatment ... #management #treatment
Pheochromocytoma - Diagnosis and Management Summary 10 percent rule = 10% of pheochromocytomas are extra-adrenal, multiple, bilateral,
Pheochromocytoma - Diagnosis ... bilateral, malignant, pediatric ... mental status changes ... disease: Management ... #Management #treatment
Hypermagnesemia - Diagnosis and Management Hypermagnesemia is a serum magnesium concentration > 2.6 mg/dL. Symptoms include hyporeflexia, hypotension,
Hypermagnesemia - Diagnosis ... and Management ... eclampsia (mothers and neonates ... insufficiency (Addison's disease ... reverse Mg-induced changes
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